A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14105462



Internal ID21286871
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:41500989..41539446hg38UCSC Ensembl
Innerchr3:41542480..41580937hg19UCSC Ensembl
Cytoband3p22.1
Allele length
AssemblyAllele length
hg3838458
hg1938458
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3110798
Supporting Variants
Samplessample395
Known GenesULK4
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14105462
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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